| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:51166126-51166560 | Common:2; Rare:87 | ||||
| chr17:51260361-51260581 | Common:3; Rare:99 | ||||
| chr17:54968595-54968814 | Common:3; Rare:100 | ||||
| chr17:56914005-56914151 | Common:1; Rare:38 | ||||
| chr17:57084956-57085335 | Common:1; Rare:127 | ||||
| chr17:57256965-57257038 | Rare:32 | ||||
| chr17:57850002-57850286 | Common:1; Rare:94 | ||||
| chr17:57988122-57988512 | Common:5; Rare:117 | ||||
| chr17:58007126-58007390 | Common:1; Rare:124 | ||||
| chr17:58219216-58219342 | Common:1; Rare:47; Clinvar:2; Clinvar (benign):4 | ||||
| chr17:58328755-58328799 | Rare:9 | ||||
| chr17:58347565-58347714 | Rare:33 | ||||
| chr17:58352125-58352495 | Common:6; Rare:140 | ||||
| chr17:58692322-58692702 | Common:2; Rare:153; Clinvar:19; Clinvar (benign):20 | ||||
| chr17:59106669-59106977 | Common:3; Rare:102; Clinvar:5; Clinvar (benign):4 |